A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18198337



Internal ID20765377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:52519074..52847331hg38UCSC Ensembl
chr19:53022327..53350584hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38328258
hg19328258
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6530477
Supporting Variants
Samples
Known GenesZNF137P, ZNF28, ZNF468, ZNF600, ZNF611, ZNF701, ZNF808, ZNF83
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18198337
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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